Clinical Trials Directory

Trials / Completed

CompletedNCT00653549

Bioavailability Study of Torsemide Tablets Under Fasting Conditions

Comparative, Randomized, Single-Dose, 2 Way Cross Over Bioavailability Study of Par Torsemide Tablets 20mg With That of Roche Demadex 1*20 mg in Healthy Subjects Under Fasting Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
26 (actual)
Sponsor
Par Pharmaceutical, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

To compare the single-dose bioavailability of Torsemide tablets with Demadex

Detailed description

To compare the single -dose bioavailability of Par Torsemide tablets 20mg with that Roche Demadex 1\*20mg tablets under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGTorsemideTablets, 20 mg, single-dose
DRUGDemadextablets, 20 mg, single-dose

Timeline

Start date
2001-04-01
Primary completion
2001-05-01
Completion
2001-05-01
First posted
2008-04-07
Last updated
2011-06-17

Source: ClinicalTrials.gov record NCT00653549. Inclusion in this directory is not an endorsement.